Citescorey = Citationsy + Citationsy-1 + Citationsy-2 + Citations y-3 / Published articlesy + Published articlesy-1 + Published articlesy-2 + Published articles y-3
Ricotti V, Jägle H, Theodorou M, Moore AT, Muntoni F, Thompson DA.(2016) Ocular and neurodevelopmental features of Duchenne muscular dystrophy: a signature of dystrophin function in the central nervous system. European Journal of Human Geneticsx ;24:562-568. View at Publisher|View at Google Scholar|View at Indexing
Goemans NM, Tulinius M, van den Hauwe M, Kroksmark AK, Buyse G.,et.al.. (2016) Long-term efficacy, safety, and pharmacokinetics of drisapersen in Duchenne muscular dystrophy: results from an open-label extension study. PloS one ;11:e0161955. View at Publisher|View at Google Scholar|View at Indexing
Li Y, Zhang S, Zhang X, Li J, Ai X, Zhang L, Yu D, Ge S, Peng Y, Chen X. (2014) Blunted cardiac beta-adrenergic response as an early indication of cardiac dysfunction in Duchenne muscular dystrophy. Cardiovascular research ;103:60-71. View at Publisher|View at Google Scholar|View at Indexing
Heslop E, Csimma C, Straub V, McCall J, Nagaraju K, Wagner KR, Caizergues D, Korinthenberg R, Flanigan KM, Kaufmann P, McNeil E. (2015)The TREAT-NMD advisory committee for therapeutics (TACT): an innovative de-risking model to foster orphan drug development. Orphanet journal of rare diseases ;10:49. View at Publisher|View at Google Scholar|View at Indexing
Geirs DP, Pottegård A, Halldórsson M, Zoëga H (2014 ) A Nationwide Study of Attentionâ€ÂDeficit/Hyperactivity Disorder Drug Use among Adults in Iceland 2003–2012. Basic & clinical pharmacology & toxicology 115: 417-422. View at Publisher|View at Google Scholar|View at Indexing
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Soto M, Abushakra S, Cummings J, Siffert J, Robert P, et al. (2015) Progress in Treatment Development for Neuropsychiatric Symptoms in Alzheimer’s Disease: Focus on Agitation and Aggression. A Report from the EU/US/CTAD Task Force. The journal of prevention of Alzheimer's disease 2:184. View at Publisher|View at Google Scholar|View at Indexing
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Toniolo RA (2016) Ensaio clínico randomizado, duplo-cego, controlado com placebo, de monoidrato de creatina como terapia adjuvante na depressão bipolar (Doctoral dissertation, Universidade de São Paulo). View at Publisher|View at Google Scholar|View at Indexing
Malheiros SR, Ribeiro DC, Alvarez MP, de Freitas BL, et.al. (2015)Motor Learning in Duchenne Muscular Dystrophy, a Literature Review. International Archives of Medicine;8. View at Publisher|View at Google Scholar|View at Indexing
Bushby K. (2015) Looking forward to new therapies: a personal perspective on the translational landscape for muscular dystrophies. Journal of Neuromuscular Diseases;2:S83. View at Publisher|View at Google Scholar|View at Indexing
López Villar E, Wu D, Cho WC, Madero L, Wang X (2014) Proteomicsâ€Âbased discovery of biomarkers for paediatric acute lymphoblastic leukaemia: challenges and opportunities. Journal of cellular and molecular medicine 18: 1239-1246. View at Publisher|View at Google Scholar|View at Indexing
Doussau A, Geoerger B, Jiménez I, Paoletti X (2016 ) Innovations for phase I dose-finding designs in pediatric oncology clinical trials. Contemporary clinical trials. 47: 217-227. View at Publisher|View at Google Scholar|View at Indexing
Buckon C, Sienko S, Bagley A, Sison-Williamson M, Fowler E, Staudt L, Heberer K, McDonald CM, Sussman M.(2016) Can Quantitative Muscle Strength and Functional Motor Ability Differentiate the Influence of Age and Corticosteroids in Ambulatory Boys with Duchenne Muscular Dystrophy?. PLoS Currents ;8. View at Publisher|View at Google Scholar|View at Indexing
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Craig TJ, Li HH, Riedl M, Bernstein JA, Lumry WR, et al. (2015 ) Characterization of anaphylaxis after ecallantide treatment of hereditary angioedema attacks. The Journal of Allergy and Clinical Immunology: In Practice 3: 206-212. View at Publisher|View at Google Scholar|View at Indexing
Bernstein JA, Moellman JJ, Collins SP, Hart KW, Lindsell CJ ( 2015 ) Effectiveness of ecallantide in treating angiotensin-converting enzyme inhibitor–induced angioedema in the emergency department. Annals of Allergy, Asthma & Immunology 114: 245-249. View at Publisher|View at Google Scholar|View at Indexing
Travlos V, Patman S, Wilson A, Simcock G, Downs J.(2016) Quality of life and psychosocial wellbeing in youth with neuromuscular disorders who are wheelchair users: A systematic review. Archives of Physical Medicine and Rehabilitation.
Pelentsov LJ, Fielder AL, Esterman AJ (2016 ) The supportive care needs of parents with a child with a rare disease: a qualitative descriptive study. Journal of pediatric nursing 31: e207-e218. View at Publisher|View at Google Scholar|View at Indexing
Vahedi L, Jabarpoor-Bonyadi M, Ghojazadeh M, Hazrati H, Rafeey M (2016) Association between outcomes and demographic factors in an Azeri Turkish population with cystic fibrosis: a cross-sectional study in Iran from 2001 through . Iranian Red Crescent Medical Journal 18. View at Publisher|View at Google Scholar|View at Indexing
Goemans N, Vanden Hauwe M, Signorovitch J, Swallow E, Song J. (2016) Individualized Prediction of Changes in 6-Minute Walk Distance for Patients with Duchenne Muscular Dystrophy. PloS one;11:e0164684. View at Publisher|View at Google Scholar|View at Indexing
Dunn AL (2016) Mapping Patient and Caregiver Involvement across the Orphan Drug Lifecycle and in Programs that Provide Access to Promising Therapies While Ensuring Prudent use of Scarce Health Care Resources (Doctoral dissertation, University of Alberta). View at Publisher|View at Google Scholar|View at Indexing
Foster CS, Kothari S, Anesi SD, Vitale AT, Chu D, et al. (2016) The Ocular Immunology and Uveitis Foundation preferred practice patterns of uveitis management. Survey of ophthalmology 61: 1-7. View at Publisher|View at Google Scholar|View at Indexing
Pigula AJ, Wu JS, Gilbertson MW, Darras BT, Rutkove SB, Anthony BW. (2016) Force-controlled ultrasound to measure passive mechanical properties of muscle in Duchenne muscular dystrophy. InEngineering in Medicine and Biology Society (EMBC), 2016 IEEE 38th Annual International Conference IEEE.. 2865-2868 View at Publisher|View at Google Scholar|View at Indexing
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Koppaka S, Shklyar I, Rutkove SB, Darras BT, Anthony BW, Zaidman CM, Wu JS. (2016) Quantitative Ultrasound Assessment of Duchenne Muscular Dystrophy Using Edge Detection Analysis. Journal of Ultrasound in Medicine;35:188918-97. View at Publisher|View at Google Scholar|View at Indexing
Rutkove SB, Kapur K, Zaidman C, Wu JS, Pasternak A, Madabusi L, et.al,. Electrical impedance myography for assessment of Duchenne muscular dystrophy. Annals of Neurology. View at Publisher|View at Google Scholar|View at Indexing
Goemans N, Tulinius M, Kroksmark AK, Wilson R, van den Hauwe M, Campion G. (2016) Comparison of ambulatory capacity and disease progression of duchenne muscular dystrophy subjects enrolled in the drisapersen DMD114673 study with a matched natural history cohort of subjects on daily corticosteroids. Neuromuscular Disorders. View at Publisher|View at Google Scholar|View at Indexing
Teng T, Xu S, Chen Q, Chen F, Li X, et al. (2016) iegesbeckia pubescens ameliorates experimental ulcerative colitis in rats by modulating PPARγ. Int J Clin Exp Med 23082-23091.